FDA Device recall Z-0759-2017
Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing…
- FDA Device
- Class II
- terminated
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing… by Teleflex Medical, citing the devices wings may become partially detached from the EFx Shield during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0759-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-16 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | US |
Product
Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.
Reason
The devices wings may become partially detached from the EFx Shield during use.
Identifiers
| code_info | Product Code: EFX002, Lot numbers: 3264480000, 3269990000, 3270100000. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0759-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.